BEUDAMED
    FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

    LAGIS ENDOSCOPIC INSTRUMENTS DISPOSABLE GRASPER

    K Number: K141902 · Decision May 26, 2015
    View on FDA
    Classifications
    1
    FEI Numbers
    573
    Registration Numbers
    573
    Same Product Code
    1391
    Applicant Total
    2
    Review Days
    316

    Basic Information

    Device Name
    LAGIS ENDOSCOPIC INSTRUMENTS DISPOSABLE GRASPER
    K Number
    K141902
    Device Class
    FDA class 2
    Clearance Type
    Traditional
    Regulation Number
    876.1500
    Medical Specialty
    Gastroenterology, Urology
    Decision
    Substantially Equivalent
    Statement or Summary
    Summary
    Applicant
    LAGIS ENTERPRISES CO, LTD.
    Date Received
    July 14, 2014
    Decision Date
    May 26, 2015
    Product Code
    GCJ
    Advisory Committee
    Gastroenterology, Urology
    Review Advisory Committee
    SU
    Third Party
    N

    Classifications

    This FDA 510(k) entry is associated with 1 FDA classification via its product code.

    Product Code Device Name
    GCJ Laparoscope, General & Plastic Surgery

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    Other Clearances by LAGIS ENTERPRISES CO, LTD.

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    K090309 LAGIS ENDOSCOPIC INSTRUMENTS